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The Journal of Allergy and Clinical Immunology|September 19, 2021
Recommendations for uniform definitions used in newborn screening for severe combined immunodeficiencyMaartje Blom, Rolf H Zetterström, Asbjørg Stray-Pedersen, et al.
Journal of Clinical Immunology|April 9, 2014
USIDNET: a strategy to build a community of clinical immunologistsKathleen E Sullivan, Jennifer M Puck, Luigi D Notarangelo, et al.
The Journal of Allergy and Clinical Immunology|March 6, 2007
Causes of death in hyper-IgE syndromeAlexandra F Freeman, David E Kleiner, Hari Nadiminti, et al.
The Journal of Allergy and Clinical Immunology|September 9, 2018
Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiencyDonald B Kohn, Michael S Hershfield, Jennifer M Puck, et al.
Frontiers in Immunology|October 10, 2022
Eosinophilic gastrointestinal disorders in patients with inborn errors of immunity: Data from the USIDNET registryPaulina Tran, Laura Gober, Elizabeth K Garabedian, et al.
Clinical Immunology (Orlando, Fla.)|November 1, 2005
HLA B44 is associated with decreased severity of autoimmune lymphoproliferative syndrome in patients with CD95 defects (ALPS type Ia)Marla M Vacek, Alejandro A Schäffer, Joie Davis, et al.
American Journal of Medical Genetics. Part A|February 26, 2004
Familial immunodeficiency with cutaneous vasculitis, myoclonus, and cognitive impairmentBeverly N Hay, Julie E Martin, Barbara Karp, et al.
Journal of Human Genetics|April 8, 2006
A novel IL2RG mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiencyRichard Kellermayer, Amy P Hsu, József Stankovics, et al.
Human Mutation|October 26, 2017
Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplificationLaia Bassaganyas, George Freedman, Dedeepya Vaka, et al.
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